ZFIN Human Disease: Fanconi renotubular syndrome 1

OBO ID: DOID:0080757

OBO ID: DOID:0080757

Term Name:	Fanconi renotubular syndrome 1	Search Ontology:
Synonyms:
Definition:	A Fanconi syndrome that has_material_basis_in heterozygous mutation in the GATM gene on chromosome 15q21. https://pubmed.ncbi.nlm.nih.gov/11090339/
References:	OMIM:134600
Ontology:	Human Disease ( DOID:0080757 )

Relationships

is a type of:	autosomal dominant disease Fanconi syndrome autosomal dominant disease Fanconi syndrome Show first 5 Terms

OTHER Fanconi renotubular syndrome 1 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
GATM	gatm	Fanconi renotubular syndrome 1	134600

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None